NDC 68788-7793 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 200 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68788-7793
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- Bupropion hydrochloride
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205794
- Marketed since
- October 13, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7793-1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-1) | Oct 13, 2020 |
| 68788-7793-2 | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-2) | Oct 13, 2020 |
| 68788-7793-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-3) | Oct 13, 2020 |
| 68788-7793-6 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-6) | Oct 13, 2020 |
| 68788-7793-8 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-8) | Oct 13, 2020 |
| 68788-7793-9 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-9) | Oct 13, 2020 |
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